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Turk J Haematol ; 18(3): 199-201, 2001 Sep 05.
Article in English | MEDLINE | ID: mdl-27264258

ABSTRACT

An abnormal hemoglobin was detected in a Balkan immigrant Turkish family. Erythrocyte morphology was similar to ß-thalassemia trait. Molecular analysis showed that the abnormal hemoglobin was Hemoglobin LeporeBoston. All affected family members were in heterozygote state and asymptomatic.

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